Tag | Content |
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EnhancerAtlas ID | HS182-12741 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:112375420-112377150 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr2:112376955-112376965 | TTCAAGTGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I111616 | chr2 | 112374341 | 112377462 |
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Enhancer Sequence | GCCACCCATG AGTAGAATGC ATACCTTACG CACGTGTGCA TGCACCTTCT CCAGGCAGGA 60 AGAGTTTCCT GTGCACCCCT CACCTCCACC CATAGGAAGA GCTATGGGAC CTACAGGAAC 120 TCCAGTGCTC CTGGGGCACT CCCAGCCTGT GGCACTGGAG TGTCACGTGG ACAACAGAGG 180 GTGGCTTTGT GGTCAGAACA GCATGGGCTC AAATCCAGCT TGGTCTTGCC TTGGCCTGCG 240 TAGCCCGGGC AGCTCTTCTG CCTCCCCCAA CCCAGGGAAG TGGGGTTGAT GTTCTGAATC 300 TGCAGGGCTC TTGGAGAAGT TACAGGGTGC CTGACACATG GGAGCCAGGC TCTGCCCACA 360 GTCACCCAGC CAGCATGTTG CAGAGCCAGG ATTTTAAATT AGATCCAGCC AGTTCCAGAA 420 TCATTACTTT TTCCGTTCCG TATGCATACC AGGCTGCCTC TTTCTAGATT ATCCTCCAAA 480 AAGCCCTGGG GAGGCGGCAG CAGCATGAGC GGCAGACAGG CGGCCAAGAA GTGAGGCCCC 540 AGACAGGGAT CTGAGCGTGA TCTTTGCCCT TGGGACGCAA GGCATCCATC CAAGAGGTCA 600 CAGAAATCAG CAGCTTTCAC CGGGAAGCCC CAAGTCCTGG GATTGGGGTG CTGAAGGGGG 660 ATCCAAAAAA AACAGTCATT GATTTGGAAG GAGATGCTGT TCTCCATCTC AGCCAGCTGT 720 TAAAGGGACA TGGATTGAAC TCCCAGGCAG GGAGGGGCAT TTTGTTTCCC TTGGCCACAT 780 CAGCATGTTT TTACAGTTGA GAGAGCAGGA GATGACTCTC CAGCCTGTGG CAGAGAGAAA 840 GTGCCCTTGG CCCAACTCCG TGGAAGATGT TCCCCACCCC CCTTCCAGGA GAAGCTCCTG 900 CTGGTGGATG CACGAACCCA GCTGGTGGCG ACACAAGGCC AGTGGGCACT CTCTGCCTTG 960 CTGAGGCCTC AGCCTCCTGG CTGCGAAGGC CCCGGGTTCC CCTCTGCAGC CAAGTCTTTA 1020 CTTCCCCTTC ACCCTGAAAA ACGTCTTCAC AGACTATCAT TCTTGGTCTC TTGACTGCCT 1080 TTCTCCGGTT TCCTTTCACA ATCCCTCAGA GATGGGACAT CTCTCCAGAG GACGCCTGGG 1140 TTGTGAGGAT CTATGGTCAG AACATTTTGG TCAATGACAG ATTACATACA CCACAGTGGC 1200 TCCCTCAGAT TATAAAGGAG CTGAATAATT CCTATCACCA AGTGACAGTG CTATGCCATC 1260 TAAGCTTGTG TAAGTACACC CTGTGATGTT CACACAATGA CGAAATCACC ATTGTTAAGT 1320 AAATGGGTTT GGGAGAAGGT TCAAACAGCT TCCACCTGCC CCACCCTTCC GTTTCCTAAG 1380 CTCAGCCATG CCTTTGGAGG GTAGCACCTT TGTTTCTTCC ACATGTCGCA AATACAGTGA 1440 CACATGACTG TATTCAGGAA CAAGGAGGCT CTGGTGCAAA AAGAACATCA TTTCCATATG 1500 TGAGTGGGTC TTCTGGGTCC ATCACAGGCA GCCAATTCAA GTGGTCCATC CGTCAACAGA 1560 ATTCTTCTTC CAGGCTCACC AGGACTTCTT CCAGCCATAG CACATAACAT CATAGCACAA 1620 CACATTACCC ACGTGTTTGT GGCAGTGCTG ACGTCAACAC ACCTCCTGCA CTGCCAGGCC 1680 TGTAAAAGTC TAGCACAATT TCATACAATA CATAATACTT GATAATAATA 1730
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